Literature DB >> 8635258

Cholesterol lowering and the use of healthcare resources. Results of the Scandinavian Simvastatin Survival Study.

T R Pedersen1, J Kjekshus, K Berg, A G Olsson, L Wilhelmsen, H Wedel, K Pyörälä, T Miettinen, T Haghfelt, O Faergeman, G Thorgeirsson, B Jönsson, J S Schwartz.   

Abstract

BACKGROUND: Advances in the treatment of cardiovascular disease have increased costs; annual cardiovascular healthcare expenditure in the United States currently exceeds $100 billion. Physicians and third-party payers need to assess the economic impact of treatments that reduce cardiovascular morbidity and mortality. METHODS AND
RESULTS: The Scandinavian Simvastatin Survival Study is a randomized, double-blind, placebo-controlled trial in which simvastatin reduced the risk of death by 30% (P=.0003) over the median follow-up period of 5.4 years in patients with previous myocardial infarction or stable angina pectoris as a result of a 42% reduction in the risk of coronary deaths (P=.00001). In the present report, data prospectively collected from hospital admissions were analyzed to evaluate the impact of simvastatin on healthcare resource use and perform a cost-minimization analysis. In the placebo group (n=2223), there were 1905 hospitalizations (average duration, 7.9 days) for acute cardiovascular events or coronary revascularization procedures among 937 patients, whereas in the simvastatin group (n=2221), there were 1403 such hospitalizations (average duration, 7.1 days) among 720 patients (all differences, P<.0001). The corresponding number of hospital days was 15089 and 9951 in the two groups, respectively (34% reduction,P<.0001). In the United States, the resulting reduction in hospitalization costs over the 5.4 years of the trial would be $3872 per patient, reducing the effective cost of simvastatin by 88% to $0.28 per day.
CONCLUSIONS: In addition to reducing mortality and morbidity in coronary heart disease patients, simvastatin markedly reduces use of hospital services, thus offsetting most of its cost.

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Year:  1996        PMID: 8635258     DOI: 10.1161/01.cir.93.10.1796

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  31 in total

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Authors:  C P Cannon
Journal:  J Thromb Thrombolysis       Date:  1999-04       Impact factor: 2.300

2.  Cost effectiveness of HMG-CoA reductase inhibitor (statin) treatment related to the risk of coronary heart disease and cost of drug treatment.

Authors:  D M Pickin; C J McCabe; L E Ramsay; N Payne; I U Haq; W W Yeo; P R Jackson
Journal:  Heart       Date:  1999-09       Impact factor: 5.994

3.  The limits to demand for health care.

Authors:  S Frankel; S Ebrahim; G Davey Smith
Journal:  BMJ       Date:  2000-07-01

4.  Cholesterol and coronary heart disease: screening and treatment.

Authors:  S Ebrahim; G D Smith; C McCabe; N Payne; M Pickin; T A Sheldon; F Lampe; F Sampson; S Ward; G Wannamthee
Journal:  Qual Health Care       Date:  1998-12

Review 5.  Resource utilisation in the management of dyslipidaemia.

Authors:  T D Szucs
Journal:  Pharmacoeconomics       Date:  1998       Impact factor: 4.981

6.  Do drugs reduce utilisation of other healthcare resources?

Authors:  Pierre-Yves Crémieux; Pierre Ouellette; Patrick Petit
Journal:  Pharmacoeconomics       Date:  2007       Impact factor: 4.981

7.  Cost effectiveness of lowering cholesterol. Full treatment of the costs and benefits is needed.

Authors:  A S Wierzbicki; T M Reynolds
Journal:  BMJ       Date:  1996-11-02

8.  Cost effectiveness of lowering cholesterol. Study greatly underestimates the cost effectiveness of statin treatment.

Authors:  J J McMurray; C E Morrison
Journal:  BMJ       Date:  1996-11-02

9.  Lipids and secondary prevention of ischaemic heart disease.

Authors:  C D Byrne; S H Wild
Journal:  BMJ       Date:  1996-11-23

10.  Resource implications and health benefits of primary prevention strategies for cardiovascular disease in people aged 30 to 74: mathematical modelling study.

Authors:  Tom Marshall; Andrew Rouse
Journal:  BMJ       Date:  2002-07-27
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